QA Associate (1 year contract)

Elanco; Occitanie; Sur place; EUR 45 000 - 60 000; Plein temps

Résumé du poste

A leading global animal health company in France is seeking a QA Associate for a 1-year contract. In this role, you will manage change controls and monitor quality management systems while supporting external inspections. A Bachelor's degree and experience in a pharmaceutical company are preferred. Join us to help make animals' lives better and enhance your career in a supportive environment.

Qualifications

• Experience in pharmaceutical company preferred.

Responsabilités

• Manage CMC change control.
• QMS monitoring and management: Deviation, CAPA, Backlog etc.
• External inspection support.
• Other QA tasks.

Connaissances

Logical thinking

Problem solving

Good English skill (reading/writing)

Formation

Bachelor's degree

Outils

Veeva

Description du poste

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Your Role: QA Associate (1 year contract):

QA 육아휴직 대체. Support the Quality assurance area of the Banwol site in compliance with the Elanco Global QualityStandard, applicable regional and/or local procedures. Contribute through continuous support andteamwork with internal clients to the business processes of the Banwol site and the delivery of quality processes, services and products to our customers. Mange the local change application of CMC change and development for domestic and export purpose.

Your Responsibilities:

• Manage CMC change control
• QMS monitoring and manage : Deviation, CAPA, Backlog etc.
• External inspection support
• Other QA tasks

What You Need to Succeed (minimum qualifications):

• Bachelor's degree
• Experience in pharmaceutical company preferred

What will give you a competitive edge (preferred qualifications):

• Veeva user preference
• Good English skill (reading / writing)
• Logical thinking & Problem solving skill